EcoDrugPlus

Protein Kinase C Epsilon

Ensembl ID : ENSAPEG00000012400
Gene Symbol: PRKCE
1 Cross references
259 Possible Orthologues:

Protein Kinase C Epsilon

Ensembl ID : ENSAPEG00000022706
Gene Symbol: PRKCE
1 Cross references
250 Possible Orthologues:

Protein Kinase C, Alpha, A

Ensembl ID : ENSAPEG00000003599
Gene Symbol: PRKCAA
2 Cross references
212 Possible Orthologues:

Protein Kinase C, Beta A

Ensembl ID : ENSAPEG00000001370
Gene Symbol: PRKCBA
1 Cross references
205 Possible Orthologues:

Protein Kinase C, Delta A

Ensembl ID : ENSAPEG00000016934
Gene Symbol: PRKCDA
1 Cross references
206 Possible Orthologues:

Protein Kinase C, Eta, A

Ensembl ID : ENSAPEG00000022646
Gene Symbol: PRKCHA
1 Cross references
223 Possible Orthologues:

Protein Kinase C, Theta

Ensembl ID : ENSAPEG00000017949
Gene Symbol: PRKCQ
1 Cross references
205 Possible Orthologues:

Protein Kinase C, Zeta

Ensembl ID : ENSAPEG00000011266
Gene Symbol: PRKCZ
1 Cross references
205 Possible Orthologues:

Protein Kinase D1

Ensembl ID : ENSAPEG00000013662
Gene Symbol: PRKD1
1 Cross references
210 Possible Orthologues:

Protein Kinase D3

Ensembl ID : ENSAPEG00000014535
Gene Symbol: PRKD3
2 Cross references
207 Possible Orthologues:

Protein Kinase D3

Ensembl ID : ENSAPEG00000019899
Gene Symbol: PRKD3
1 Cross references
218 Possible Orthologues:

Protein Kinase, Dna-Activated, Catalytic Subunit

Ensembl ID : ENSAPEG00000008072
Gene Symbol: PRKDC
1 Cross references
187 Possible Orthologues:


PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains. Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).